Gerald Goh

发表

Mutational landscape of MCPyV-positive and MCPyV-negative Merkel cell carcinomas with implications for immunotherapy

T. Chan, R. Lifton, N. Riaz, 2015, Oncotarget.

Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma

Matthew J. Davis, S. Ariyan, K. Kidd, 2012, Nature Genetics.

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

Murim Choi, R. Lifton, U. Scholl, 2015, eLife.

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

Annabelle L. Fonseca, S. Mane, S. Libutti, 2013, Nature Genetics.

Exome sequencing identifies recurrent somatic RAC 1 mutations in melanoma

Matthew J. Davis, S. Ariyan, K. Kidd, 2016 .

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

PRKACA mutations in cortisol-producing adenomas and adrenal hyperplasia: a single-center study of 60 cases.

U. Scholl, G. Goh, M. Schott, 2015, European journal of endocrinology.

Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors

D. Dietrich, Murim Choi, R. Lifton, 2014, Nature Genetics.

Clonal Evolutionary Analysis during HER2 Blockade in HER2-Positive Inflammatory Breast Cancer: A Phase II Open-Label Clinical Trial of Afatinib +/- Vinorelbine

Charles Swanton, Gerald Goh, Imjai Chitapanarux, 2016, PLoS medicine.

Genomic landscape of cutaneous T cell lymphoma

D. Schatz, R. Bjornson, T. Boggon, 2015, Nature Genetics.

Fc-Optimized Anti-CD25 Depletes Tumor-Infiltrating Regulatory T Cells and Synergizes with PD-1 Blockade to Eradicate Established Tumors

Nicolai J. Birkbak, Angela E. Leek, R. Booton, 2017, Immunity.

Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

S. Scherer, J. Sutcliffe, D. Geschwind, 2009, PloS one.

Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing.

S. Mane, C. Larsson, D. Rimm, 2015, Human molecular genetics.

Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases

Murim Choi, Gerald Goh, Murim Choi, 2012, Genomics & informatics.

Identification of a gain-of-function STAT3 mutation (p.Y640F) in lymphocytic variant hypereosinophilic syndrome.

R. Lifton, G. Goh, Chen Wang, 2016, Blood.

Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma.

Simion I. Chiosea, R. Herbst, Lin Wang, 2016, The Journal of clinical investigation.

Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma.

Simion I. Chiosea, R. Herbst, Lin Wang, 2016, The Journal of clinical investigation.

Title Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma

Simion I. Chiosea, R. Herbst, Lin Wang, 2015 .

Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene

Jenny Welander, Gerald Goh, Stefano Caramuta, 2015, Genes, chromosomes & cancer.

Increased Levels of Macrophage Inflammatory Proteins Result in Resistance to R5-Tropic HIV-1 in a Subset of Elite Controllers

Samit R. Joshi, M. Kozal, E. Fikrig, 2015, Journal of Virology.

DNA replication stress mediates APOBEC3 family mutagenesis in breast cancer

R. Harris, Emily K. Law, N. McGranahan, 2016, Genome Biology.

Clonal Evolutionary Analysis during HER2 Blockade in HER2-Positive Inflammatory Breast Cancer: A Phase II Open-Label Clinical Trial of Afatinib +/- Vinorelbine.

Sung-Bae Kim, C. Swanton, S. Johnston, 2016 .

Multiple Recurrent De Novo Copy Number Variations , Including Duplications of the 7 q 11 . 23 Williams-Beuren Syndrome Region , Are Associated with Autism

Rebecca, Michael J. DiCola, Stephan J Sanders, 2011 .

Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype

Annabelle L. Fonseca, G. Kristiansen, D. Dietrich, 2015, Clinical endocrinology.

Effector CD4+ T Cell Expression Signatures and Immune-Mediated Disease Associated Genes

Judy H. Cho, John P. Ferguson, Hongyu Zhao, 2012, PloS one.

Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinoma.

Annabelle L. Fonseca, S. Mane, C. Larsson, 2015, The Journal of clinical endocrinology and metabolism.

Shifting patterns of genomic variation in the somatic evolution of papillary thyroid carcinoma

R. Lifton, C. Nelson-Williams, G. Goh, 2016, BMC Cancer.

Chromosome 19 amplification correlates with advanced disease in adrenocortical carcinoma.

G. Goh, A. Stenman, R. Korah, 2016, Surgery.

Intratumoural evolutionary landscape of high-risk prostate cancer: the PROGENY study of genomic and immune parameters

Nicolai J. Birkbak, Z. Szallasi, M. Gerlinger, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma.

Simion I. Chiosea, R. Herbst, Lin Wang, 2016, The Journal of clinical investigation.

Computational Methods for Analysis of Tumor Clonality and Evolutionary History.

G. Wilson, G. Goh, N. Mcgranahan, 2018, Methods in molecular biology.